CORONA PLUS- hand sanitizer liquid 
ALTERNATIVE UNIVERSAL MEDICINE INC

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

----------

Coroa Plus Hand Sanitizer Registration

Product Application / Dosage

Place enough product on hands to cover all surfaces. Rub hands together until dry.

Keep Out Of Reach Of Children

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away. Do not use in/on children less than 2 month of age. Supervise children under 6 years of age when using this product to avoid swallowing.

Warnings Section

For external use only: hands. Flammable. Keep away from fire or flame. When using the product keep out of eyes, ears, and mouth. In case of contact with eyes, rinse thoroughly with water. Stop use and ask a doctor if irritation or rash occurs. These may be signs of serious condition. Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away. Do not use in/on children less than 2 month of age. Do not use on open wounds.

Inactive Ingredient Section

Inactive ingredients

Glycerin, Hydrogen peroxide, Purified water

Indication And Usage

Uses

Hand Sanitizer to help reduce bacteria on the skin that potentially can cause disease. Recommender for repeated use.

Warnings

For external use only: hands. Flammable. Keep away from fire or flame. When using the product keep out of eyes, ears, and mouth. In case of contact with eyes, rinse thoroughly with water. Stop use and ask a doctor if irritation or rash occurs. These may be signs of serious condition.

Purpose Section

Purpose

Antiseptic

Active Ingredient

Active Ingredients

Ethyl Alcohol 86%vv

Corona Plus Package Label

3.78 ml Corona Plus Back LabelFront Label Product Lable - NDC - 79441-299-01

Front and Back

CORONA PLUS 
hand sanitizer liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:79441-299
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL86.18 mL  in 100 mL
Inactive Ingredients
Ingredient NameStrength
GLYCERIN (UNII: PDC6A3C0OX) 4.17 mL  in 100 mL
HYDROGEN PEROXIDE (UNII: BBX060AN9V) 1.5 mL  in 100 mL
WATER (UNII: 059QF0KO0R) 8.15 mL  in 100 mL
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:79441-299-013780 mL in 1 BOTTLE; Type 0: Not a Combination Product08/15/2020
2NDC:79441-299-02473 mL in 1 BOTTLE; Type 0: Not a Combination Product10/27/2020
3NDC:79441-299-03946 mL in 1 BOTTLE; Type 0: Not a Combination Product10/27/2020
4NDC:79441-299-04236.5 mL in 1 BOTTLE; Type 0: Not a Combination Product10/27/2020
5NDC:79441-299-05118.25 mL in 1 BOTTLE; Type 0: Not a Combination Product10/27/2020
6NDC:79441-299-0659.125 mL in 1 BOTTLE; Type 0: Not a Combination Product10/27/2020
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333A08/15/2020
Labeler - ALTERNATIVE UNIVERSAL MEDICINE INC (024341671)
Establishment
NameAddressID/FEIBusiness Operations
ALTERNATIVE UNIVERSAL MEDICINE INC024341671manufacture(79441-299)

Revised: 10/2020
Document Id: b2aa2cfe-2c77-92be-e053-2995a90a8417
Set id: ab96c10e-b1a2-2d7d-e053-2995a90a4f74
Version: 2
Effective Time: 20201027
 
ALTERNATIVE UNIVERSAL MEDICINE INC